Canonical Allele Identifier: CA352652392

Gene: COL7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48572152C>A , CM000665.2:g.48572152C>A	GRCh38
NC_000003.11:g.48609585C>A , CM000665.1:g.48609585C>A	GRCh37
NC_000003.10:g.48584589C>A	NCBI36
NG_007065.1:g.28101G>T , LRG_286:g.28101G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000094.4:c.6998G>T MANE Select	NP_000085.1:p.Gly2333Val
ENST00000681320.1:c.6998G>T MANE Select	ENSP00000506558.1:p.Gly2333Val
NM_000094.3:c.6998G>T , LRG_286t1:c.6998G>T	NP_000085.1:p.Gly2333Val
ENST00000328333.12:c.6998G>T	ENSP00000332371.8:p.Gly2333Val
ENST00000487017.5:n.2915G>T
XM_011533336.1:c.7025G>T	XP_011531638.1:p.Gly2342Val
XM_011533337.1:c.6998G>T	XP_011531639.1:p.Gly2333Val
XM_011533338.1:c.7025G>T	XP_011531640.1:p.Gly2342Val
XM_011533339.1:c.7025G>T	XP_011531641.1:p.Gly2342Val
XM_011533340.1:c.7025G>T	XP_011531642.1:p.Gly2342Val
XM_011533341.1:c.7025G>T	XP_011531643.1:p.Gly2342Val
XM_011533342.1:c.7025G>T	XP_011531644.1:p.Gly2342Val
XM_017005688.1:c.6998G>T	XP_016861177.1:p.Gly2333Val
XM_017005689.1:c.6998G>T	XP_016861178.1:p.Gly2333Val
XM_017005690.1:c.6998G>T	XP_016861179.1:p.Gly2333Val
XM_017005691.1:c.6998G>T	XP_016861180.1:p.Gly2333Val
XM_017005692.1:c.6998G>T	XP_016861181.1:p.Gly2333Val
XR_001740003.1:n.7034G>T
XR_001740004.1:n.7034G>T
XR_001740005.1:n.7034G>T
XR_001740006.1:n.7034G>T
XR_001740007.1:n.7034G>T
XR_001740008.1:n.7044G>T
XR_940369.1:n.7061G>T
XR_940370.1:n.7061G>T
XR_940371.1:n.7061G>T
XR_940372.1:n.7061G>T
XR_940373.1:n.7061G>T
XR_940374.1:n.7071G>T